Caspase-dependent chemotherapy-induced death of glioma cells requires mitochondrial cytochrome c release

被引:27
作者
Glaser, T [1 ]
Weller, M [1 ]
机构
[1] Univ Tubingen, Dept Neurol, Mol Neurooncol Lab, D-7400 Tubingen, Germany
关键词
caspases; cytochrome c; chemotherapy; glioma; apoptosis;
D O I
10.1006/bbrc.2001.4349
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chemotherapeutic drug-induced apoptosis of human malignant glioma cells involves the death receptor-independent activation of caspases other than caspases 3 or 8 (Glaser et at, Oncogene 18, 5044-5053, 1999), Here, we report that caspases 1, 2, 3, 7, 8, and 9 are constitutively expressed in most human malignant glioma cell lines. Cytotoxic drug-induced apoptosis involves delayed activation of caspases 2, 7, and 9, but not 8 and 3, and is blocked by a broad spectrum caspase inhibitor, zVAD-fmk, Cytochrome c release from mitochondria precedes caspase activation during drug-induced apoptosis and is unaffected by zVAD-fmk or ectopic expression of the viral caspase inhibitor, crm-A In contrast, ectopic expression of BCL-X-L prevents drug-induced cytochrome c release, caspase activation and cell death. Thus, cancer chemotherapy targets the mitochondrial, caspase-dependent death pathway in human malignant glioma cells. (C) 2001 Academic Press.
引用
收藏
页码:322 / 327
页数:6
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